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Journal Abstract Search

351 related items for PubMed ID: 19726938

  • 1. Neuro-ophthalmologic features of spinocerebellar ataxia type 7.
    Miller RC, Tewari A, Miller JA, Garbern J, Van Stavern GP.
    J Neuroophthalmol; 2009 Sep; 29(3):180-6. PubMed ID: 19726938
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  • 2. Ophthalmic features of spinocerebellar ataxia type 7.
    Manrique RK, Noval S, Aguilar-Amat MJ, Arpa J, Rosa I, Contreras I.
    J Neuroophthalmol; 2009 Sep; 29(3):174-9. PubMed ID: 19726937
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  • 3. Macular dysfunction and morphology in spinocerebellar ataxia type 7 (SCA 7).
    Hugosson T, Gränse L, Ponjavic V, Andréasson S.
    Ophthalmic Genet; 2009 Mar; 30(1):1-6. PubMed ID: 19172503
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  • 4. Two patients with spinocerebellar ataxia type 7 presenting with profound binocular visual loss yet minimal ophthalmoscopic findings.
    Thurtell MJ, Fraser JA, Bala E, Tomsak RL, Biousse V, Leigh RJ, Newman NJ.
    J Neuroophthalmol; 2009 Sep; 29(3):187-91. PubMed ID: 19726939
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  • 7. [The value of multifocal ERG in diagnosis of discrete macular dystrophies].
    Zaninetti M, Safran AB.
    Klin Monbl Augenheilkd; 2004 May; 221(5):379-82. PubMed ID: 15162285
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  • 8. Foveal cone dysfunction syndrome.
    ten Hove MW, Siatkowski RM, Smith JL.
    J Neuroophthalmol; 1998 Mar; 18(1):9-14. PubMed ID: 9532531
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  • 12. Anatomical and functional characteristics in atrophic maculopathy associated with spinocerebellar ataxia type 7.
    Ahn JK, Seo JM, Chung H, Yu HG.
    Am J Ophthalmol; 2005 May; 139(5):923-5. PubMed ID: 15860307
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  • 13. Maculopathy and spinocerebellar ataxia type 1: a new association?
    Lebranchu P, Le Meur G, Magot A, David A, Verny C, Weber M, Milea D.
    J Neuroophthalmol; 2013 Sep; 33(3):225-31. PubMed ID: 23584155
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  • 15. Evidence for a common Spinocerebellar ataxia type 7 (SCA7) founder mutation in Scandinavia.
    Jonasson J, Juvonen V, Sistonen P, Ignatius J, Johansson D, Björck EJ, Wahlström J, Melberg A, Holmgren G, Forsgren L, Holmberg M.
    Eur J Hum Genet; 2000 Dec; 8(12):918-22. PubMed ID: 11175279
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  • 19. Spinocerebellar ataxia type 7 mimicking Kearns-Sayre syndrome: a clinical diagnosis is desirable.
    Gupta SN, Marks HG.
    J Neurol Sci; 2008 Jan 15; 264(1-2):173-6. PubMed ID: 17720198
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